DEERFIELD, Ill.--(BUSINESS WIRE)-- Baxter International Inc. (NYSE: BAX), a leader in innovative technology for medication delivery, today announced the U.S. Food and Drug Administration (FDA) ...

Designed with Exclusive New Features for Bi-Directional Electronic Medical Records Integration Including Auto-Programming and Auto-Documentation Offers Both English and French Language Options and ...

Device manufacturer Baxter released an Urgent Safety Communication last week about the company's Spectrum V8 and Spectrum IQ infusion pumps, citing potential compromised medication delivery caused by ...

Errors in the setup or management of some of Baxter International’s infusion pumps could result in overlooked blockages in the pumps, potentially leading to serious injury or even death, the ...

Baxter Healthcare has once again found itself in the depths of a Class I recall for its infusion pump systems. Recently announcing the recall, the company reported that its Sigma Spectrum Infusion ...

Baxter International Inc. announced today it has issued an Urgent Medical Device Correction for all Spectrum IQ infusion pumps to reinforce important safety information when customers implement ...

Baxter International Inc. announced today it has issued an Urgent Medical Device Correction for Spectrum V8 and Spectrum IQ infusion pumps in the U.S. and Puerto Rico that have been upgraded to ...

The FDA labeled 22,769 Baxter drug infusion devices as a Class I recall after receiving reports of false upstream occlusion alarms, which can delay therapy. The two infusion pumps, SIGMA Spectrum ...

Baxter has issued a correction for its Novum IQ Large Volume Pumps and Novum IQ Syringe Pumps. All Novum large volume and syringe pumps have a software anomaly that ...

DEERFIELD, Ill.--(BUSINESS WIRE)--Baxter International Inc. (NYSE: BAX), a leader in innovative technology for medication delivery, today announced the U.S. Food and Drug Administration (FDA) ...